AI Article Synopsis

  • Purine homeostasis is maintained through a conserved metabolic network across various organisms, but the regulation of purine biosynthesis in humans is not well understood.
  • A deficiency in the enzyme adenylosuccinate lyase (ADSL) is linked to serious muscular and neuronal symptoms, prompting researchers to investigate its mechanisms using a metazoan model organism.
  • The study reveals that ADSL is crucial for developmental timing, maintaining germline stem cells, and muscle integrity, indicating distinct roles of the purine metabolic network in different biological processes.

Article Abstract

Purine homeostasis is ensured through a metabolic network widely conserved from prokaryotes to humans. Purines can either be synthesized , reused, or produced by interconversion of extant metabolites using the so-called recycling pathway. Although thoroughly characterized in microorganisms, such as yeast or bacteria, little is known about regulation of the purine biosynthesis network in metazoans. In humans, several diseases are linked to purine metabolism through as yet poorly understood etiologies. Particularly, the deficiency in adenylosuccinate lyase (ADSL)-an enzyme involved both in the purine and recycling pathways-causes severe muscular and neuronal symptoms. In order to address the mechanisms underlying this deficiency, we established as a metazoan model organism to study purine metabolism, while focusing on ADSL. We show that the purine biosynthesis network is functionally conserved in Moreover, (the gene encoding ADSL in ) is required for developmental timing, germline stem cell maintenance and muscle integrity. Importantly, these traits are not affected when solely the pathway is abolished, and we present evidence that germline maintenance is linked specifically to ADSL activity in the recycling pathway. Hence, our results allow developmental and tissue specific phenotypes to be ascribed to separable steps of the purine metabolic network in an animal model.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456310PMC
http://dx.doi.org/10.1534/genetics.118.301062DOI Listing

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